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NCT ID: NCT01161394 Completed - Inflammation Clinical Trials

Effect of Pioglitazone on Oxidative Load, Inflammatory End-Points and Vascular Reactivity in Obese Non-Diabetic Patients: A Dose Ranging Study

Start date: n/a
Phase: Phase 4
Study type: Interventional

Pioglitazone decreases oxidative load, inflammatory end points and improves vascular reactivity in obese patients in a dose dependent manner and that this effect is independent of its glucose lowering effects.

NCT ID: NCT01161602 Completed - Clinical trials for Gastroesophageal Reflux Disease

A Study to Evaluate the Safety, Tolerability and Pharmacodynamics of Pumosetrag in Patients With Gastroesophageal Reflux Disease (GERD)

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if pumosetrag is effective in treating Gastroesophageal Reflux Disease (GERD) symptoms in patients who have a history of GERD symptoms and are currently taking an acid suppression therapy, such as a Proton Pump Inhibitor (PPI).

NCT ID: NCT01164748 Completed - Breast Cancer Clinical Trials

Lymphatic Mapping After Previous Breast Surgery

LABS
Start date: n/a
Phase: N/A
Study type: Observational

Rationale: Like in primary breast cancer, prognosis in recurrent breast cancer is correlated with regional lymph node status. Therefore, axillary staging may be warranted in patients with recurrent disease and intact axillary nodes, although this has not been described in guidelines yet. The lymphatic drainage pathways in the breast and/or axilla could have been changed due to prior surgery and/or radiotherapy. These aberrant drainage pathways could be detected with lymphatic mapping and sentinel node biopsy (SNB), leading to a more accurate staging. Objective: To assess the technical feasibility of lymphoscintigraphy after prior breast surgery. A second goal is to investigate whether or not previous breast surgery (with or without radiotherapy) significantly changes the lymphatic drainage pathways of the breast.

NCT ID: NCT01165606 Completed - Clinical trials for Mechanical Ventilation

Effects of Respiratory Physiotherapy in Critically Ill Patients Ventilated for More Than 48 Hours

Start date: n/a
Phase: N/A
Study type: Interventional

This study aimed to determine the impact of providing chest physiotherapy on the duration of mechanical ventilation, intensive care length of stay, intensive care and hospital mortality in mechanically ventilated patients.

NCT ID: NCT01169792 Completed - Breast Neoplasms Clinical Trials

Study of Cytochrome P450 Polymorphisms (CYP2D6, CYP3A4/5 and CYP2C19) in Breast Cancer Patients

Start date: n/a
Phase: N/A
Study type: Observational

The genetic polymorphisms of the cytochrome P450 may influence on the metabolism of tamoxifen. The investigators want to - evaluate the frequency or incidence of the genetic polymorphisms of cytochrome P450 subfamilies(CYP2D6, CYP3A4/5 and CYP2C19) in breast cancer patients, and - analyze the association between the genetic polymorphisms of cytochrome P450 subfamilies and clinical outcomes in breast cancer patients treated by adjuvant tamoxifen therapy.

NCT ID: NCT01171079 Completed - Thyroidectomy Clinical Trials

Use of an Oxidized Regenerated Cellulose After Thyroid Surgery: A Prospective, Randomized Study

ORC
Start date: n/a
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effects and safety of oxidized, regenerated cellulose as an absorbable adhesion barrier after thyroidectomy.

NCT ID: NCT01173250 Completed - Ulcerative Colitis Clinical Trials

Is Diverting Ileostomy Necessary in Stapled Ileoanal Pouch?

Start date: n/a
Phase: N/A
Study type: Interventional

Total proctocolectomy with ileal pouch anal anastomosis is the first choice surgical operation for management of ulcerative colitis and familial adenomatous polyposis. The addition of diverting ileostomy may reduce septic complications. In this randomized study the investigators compare two groups of patients with stapled ileoanal pouch one of them had diverting ileostomy and in the other this step is omitted.

NCT ID: NCT01176305 Completed - Clinical trials for Venous Thromboembolism

Venous Thromboembolism in Pregnant and Puerperal Women in Denmark 1995-2005

Start date: n/a
Phase: N/A
Study type: Observational

The purpose of this study is to describe the incidence of thromboembolic events in relation to pregnancy and when in pregnancy and the puerperal period.

NCT ID: NCT01176331 Completed - Vitrectomy Clinical Trials

Outcomes of 20 and 23-gauge Combined Transconjunctival Pars Plana Vitrectomy

Start date: n/a
Phase: Phase 4
Study type: Observational

In a retrospective study, a combined 20 and 23-gauge pars plana vitrectomy procedure was performed in 21 eyes for various indications and proposed as a transition procedure to 23-gauge transconjunctival vitrectomy. Through use of combination of procedures postoperative complications, surgical trauma and healing time was decreased; operating time was reduced; costs were decreased.

NCT ID: NCT01179035 Completed - Clinical trials for Health Services Research, Prisons, Delivery of Health Care, Vulnerable Populations, Community Health Aides

Evaluation of Transitions Clinic: A Post-Release Clinic for Recently Released Parolees With Chronic Medical Conditions

Start date: n/a
Phase: N/A
Study type: Interventional

The purpose of this study is to study the effectiveness of the Transitions Clinic, a post-release clinic for parolees with chronic medical conditions, in achieving increased primary care engagement, lower rates of inappropriate hospitalizations, psychiatric emergency service and emergency department use, and decreased recidivism. We hypothesize that subjects receiving parolee-targeted care in the Transitions Clinic will have increased rates of non-emergency department ambulatory care and outpatient mental health care, lower rates of hospitalization, psychiatric emergency service (PES) utilization, emergency department (ED) utilization, decreased total hospital length of stay, and decreased recidivism compared to patients receiving primary care from other safety-net providers.